Labshake search
Citations for Illumina :
4351 - 4400 of 10000+ citations for Creatinine Serum Low Sample Volume Kit 384 well Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Molecular Biology 2022Quote: ... prior to mixing of multiplexed libraries diluted to 2nM concentration (calculated based the on Qubit dsDNA HS Assay Kit) for sequencing using the NextSeq 500/550 v2.5 kit (Illumina, 75bp single-end reads). Finally ...
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bioRxiv - Cancer Biology 2022Quote: ... RNA-seq libraries were generated from 500 ng of total RNA using the TruSeq Stranded mRNA Library Prep Kit and TruSeq RNA Single Indexes kits A and B (Illumina, San Diego, CA), according to the manufacturer’s instructions ...
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bioRxiv - Microbiology 2022Quote: ... 20-100 ng genomic DNA was used to prepare WGS libraries using the Illumina DNA Prep Kit (formerly known as Illumina Nextera Flex Kit) using a modified protocol that utilized 5x reduced quantities of tagmentation reagents per prep ...
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bioRxiv - Molecular Biology 2022Quote: ... RNA-Seq libraries were generated from 100 to 300 ng of RNA using TruSeq Stranded Total RNA Library Prep Gold kit and TruSeq RNA Single Indexes kits A and B (Illumina, San Diego, CA), according to manufacturer’s instructions ...
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bioRxiv - Cancer Biology 2024Quote: ... Total RNA-Seq libraries were generated from 700 ng of total RNA using TruSeq Stranded Total RNA Library Prep Gold kit and TruSeq RNA Single Indexes kits A and B (Illumina, San Diego, USA), according to manufacturer’s instructions ...
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bioRxiv - Neuroscience 2024Quote: ... RNA-Seq libraries were generated from 200 ng of total RNA using TruSeq Stranded mRNA Library Prep Kit and TruSeq RNA Single Indexes kits A and B (Illumina, San Diego, CA), according to the manufacturer’s instructions ...
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bioRxiv - Genomics 2024Quote: ... and the final sequencing library was amplified utilizing the KAPA HiFi HotStart Uracil+ ReadyMix PCR Kit along with index primers from the Nextera XT Index Kit (Illumina, FC-131-1001). The amplification protocol involved an initial step at 98°C for 45 seconds ...
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bioRxiv - Genomics 2024Quote: ... Total RNA-seq libraries were then generated using TruSeq Stranded mRNA Library Prep kit and TruSeq RNA Single Indexes kits A and B (Illumina, San Diego, CA) omitting the poly-A selection step and starting from the fragmentation step ...
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bioRxiv - Microbiology 2023Quote: ... We prepared DNA libraries employing the Nextera XT library preparation kit and the Nextera XT v2 index kit (Illumina, San Diego, CA, USA). The library was sequenced on a HiSeq4000 (Illumina ...
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bioRxiv - Biophysics 2023Quote: ... The DNA concentration was measured using the Qubit dsDNA BR assay kit and sequenced using a HiSeq SBS v4 50 cycle kit (Illumina FC-401-4002) and HiSeq SR Cluster Kit v4 (Illumina GD-401-4001 ...
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bioRxiv - Microbiology 2023Quote: ... Library preparation was performed using an Illumina Nextera DNA Flex Library Prep Kit and multiplexing at 96-plex on a NextSeq 500 System using the Mid-Output Kit (Illumina, San Diego, USA). Resulting fastq files underwent a quality check ...
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bioRxiv - Cell Biology 2023Quote: ... Library preparation is performed with or without amplification (Nextera® DNA Flex Library Prep kit or TruSeq® DNA PCR-Free kit, ILLUMINA®), either through automation (MICROLAB Star® ...
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bioRxiv - Biochemistry 2023Quote: ... The DNA concentration was measured using the Qubit dsDNA BR assay kit and sequenced using a HiSeq SBS v4 50 cycle kit (Illumina FC-401-4002) and HiSeq SR Cluster Kit v4 (Illumina GD-401-4001 ...
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bioRxiv - Molecular Biology 2020Quote: Libraries of eDNA and iDNA samples at 50 ng μL−1 were sequenced using a MiSeq PE300 benchtop sequencer (Illumina, USA). Library preparation was done with a TruSeq DNA PCR-Free kit (LT Lib PREP KT-ST B PhiX control v3) ...
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bioRxiv - Genetics 2021Quote: ... were prepared from RNA samples with a RIN (RNA integrity number) above 8 using the strand-specific TruSeq™ RNA-seq library (Illumina), and 150 bp paired-end read sequencing over three lanes of the Illumina HiSeq4000 sequencing platform was performed at the Norwegian Sequencing Centre ...
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bioRxiv - Genomics 2020Quote: ... CNV analysis was performed on a combined cohort of 130 sequenced hESC lines and a control cohort consisting of 243 human samples from primary blood or lymphoblastoid cell lines (LCL) that had undergone WGS on the same platform (Illumina HiSeqX) and to similar depth as the hESC lines (Pato et al. ...
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bioRxiv - Molecular Biology 2021Quote: ... the mRNA expression data in z-scores relative to all samples (log microarray) carried out on the Illumina HT-12 v3 platform (Illumina_Human_WG-v3) (32 ...
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bioRxiv - Evolutionary Biology 2022Quote: ... 150bp paired-end sequencing of each sample was performed on an Illumina NovaSeq 6000 platform (Illumina Inc., San Diego, CA, USA). Library quality was assessed on the Agilent Bioanalyzer 2100 system (Agilent Technologies ...
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bioRxiv - Genomics 2020Quote: ... a total of 936 DNA samples were sent for genome-wide SNP genotyping using the Infinium Global Screening Array (GSA) with Shared Custom Content (Illumina Inc.). After extensive QC and imputation ...
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bioRxiv - Microbiology 2019Quote: ... DNA samples were library prepared for NGS using the Illumina MiSeq platform (2 x 300 bp; Illumina, San Diego, CA, USA) by Ohio State University Molecular and Cellular Imaging Center.
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bioRxiv - Cell Biology 2019Quote: ... 10 samples were sequenced with 151 bp paired-end reads on a single lane of NextSeq 500 (Illumina, San Diego, CA) at the Stanford Functional Genomics Facility.
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bioRxiv - Neuroscience 2019Quote: ... allowing for 10 ‘barcodes’ per sample and sequenced on Illumina HiSeq 2500 or NextSeq 500 platforms (Illumina, San Diego, CA, USA).
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bioRxiv - Cancer Biology 2019Quote: We assessed genome-wide DNA methylation in seven tumor samples with the Illumina Methylation EPIC microarray (Illumina, San Diego, CA, USA). DNA methylation assays were performed as per the standard manufacturer’s protocol by MWG (Aros – Denmark) ...
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bioRxiv - Neuroscience 2019Quote: Buccal swab and saliva samples were collected for DNA extraction followed by genome-wide genotyping using the “Global Screening Array” (Illumina, Inc). For a full description of genotyping and post-genotyping methods ...
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bioRxiv - Genomics 2019Quote: We generated a whole-genome paired-end library with the Illumina TruSeq DNA Sample Prep v2 (Illumina, San Diego, CA, USA), selecting for a mean fragment length of 450 bp with the SPRIselect reagent kit (Beckman Coulter ...
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bioRxiv - Neuroscience 2021Quote: ... and 80 million reads for each of the 24 samples of 3xTg-AD and C57BL/6×129/Sv mice in a fraction of a sequencing lane on HiSeq2000 (Illumina, Inc) following the manufacturer’s protocol ...
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bioRxiv - Biochemistry 2020Quote: ... and 1 μL of 0.25 μM primer (RTB000 and RTB001 in Table S5 for the no modification and 1M7 samples respectively, with these sequences adding an index sequence and Illumina adapter). The reaction volume was brought to 15 μL ...
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bioRxiv - Cell Biology 2021Quote: ... Sample RNA was sent to Genewiz (South Plainfield, NJ) for commercial sequencing (Total RNA, Illumina HiSeq 4000, paired end, 150bp reads). Strand specific libraries were prepped with the Ribo-zero Gold HMR and TruSeq ® Stranded Total RNA Library Prep Human/Mouse/Rat.
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bioRxiv - Molecular Biology 2021Quote: ... Sample libraries (20 nM) were subjected to multiplex next generation sequencing using an Illumina HiSeq4000 (Illumina Inc.; San Diego, CA, USA). Quality control on raw reads was performed using FASTQC ...
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bioRxiv - Cell Biology 2021Quote: Sample libraries were prepared for Illumina sequencing by denaturing and diluting the libraries per manufacturer’s protocol (Illumina, San Diego, CA, USA). All samples were pooled into one sequencing pool ...
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bioRxiv - Neuroscience 2020Quote: ... Samples were sequences with Illumina (TruSeq® Stranded mRNA Library Prep, single reads of 100bp length, Illumina®, San Diego, USA). Between 26 and 48 million reads were obtained per sample ...
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bioRxiv - Microbiology 2021Quote: Protocols for preparing samples for sequencing were specifically designed for the Illumina iSeq 100 System (Illumina Inc., San Diego, CA, USA), a portable ...
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bioRxiv - Neuroscience 2020Quote: ... Samples were processed according to the standard 10x Chromium 3’ workflow and pooled before sequencing over two lanes (Illumina HiSeq 4000).
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bioRxiv - Developmental Biology 2022Quote: ... cDNA samples were processed and RNA-sequenced on a Illumina HiSeq® 2000 Sequencing platform (Illumina Inc, San Diego, CA, USA), according to the manufacturer’s instructions ...
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bioRxiv - Plant Biology 2019Quote: ... The isolated total RNA (0.3 μg) was used to prepare samples using TruSeq® Stranded mRNA (Illumina, San Diego, CA, USA) according to the manufacturer’s instructions ...
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bioRxiv - Cancer Biology 2020Quote: ... libraries are pooled at 8 samples per lane and sequenced on an Illumina HiSeq 4000 sequencer (Illumina Inc, San Diego, CA) at PE 2×100 cycles ...
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bioRxiv - Cancer Biology 2019Quote: ... libraries are pooled at 8 samples per lane and sequenced on an Illumina HiSeq 4000 sequencer (Illumina Inc, San Diego, CA) at PE 2×100 cycles ...
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bioRxiv - Evolutionary Biology 2019Quote: We assessed input gDNA quantity using Qubit and normalised the samples to 20ng/ul as described in TruSeq®DNA PCR-Free Library Prep Reference Guide (#FC-121-3001, Illumina) prior fragmentation to 350bp with Covaris S2 ...
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bioRxiv - Neuroscience 2020Quote: ... The resulting libraries were sequenced using HiSeqTM 2500 Illumina platform to obtain a minimum 12GB raw data per sample (Illumina, USA). A brief experimental workflow was illustrated using BioRender software (Figure 1b).
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bioRxiv - Cancer Biology 2021Quote: Genome-wide DNA methylation profiling of all samples was performed using the Infinium MethylationEPIC (EPIC) BeadChip (Illumina, San Diego, CA, USA) or Infinium HumanMethylation450 (450k ...
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bioRxiv - Pharmacology and Toxicology 2021Quote: ... sequence libraries were prepared for each sample using TruSeq Stranded mRNA Library Prep/TruSeq RNA Single Indexes Set A & Set B (Illumina, Inc.). For sequencing ...
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bioRxiv - Evolutionary Biology 2020Quote: ... Library preparation was carried out as described in the Illumina Nextera XT Sample Preparation Guide (Illumina, Inc., San Diego, CA, USA). 150 pg of input cDNA were tagmented by the Nextera XT transposome ...
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bioRxiv - Evolutionary Biology 2020Quote: ... Strand-specific library preparation (one library per sample) and paired-end (150 + 150 bp) Illumina sequencing (Illumina HiSeq 3000, 5 lanes) was then performed at the Finnish Functional Genomics Center (FFCG) ...
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bioRxiv - Microbiology 2020Quote: ... Libraries were prepared according to the JGI’s iTag library construction standard operating protocol (SOP) v.1.0 (https://1ofdmq2n8tc36m6i46scovo2e-wpengine.netdna-ssl.com/wp-content/uploads/2019/07/iTag-Sample-Preparation-for-Illumina-Sequencing-SOP-v1.0.pdf). We briefly summarize their protocol here ...
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bioRxiv - Immunology 2021Quote: ... Samples were sequenced on an Illumina Novaseq 6000 S4 flowcell (67 bp read 1 and 140 bp read 2) (Illumina, USA) to a depth of approximately 100,000 reads per cell ...
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bioRxiv - Immunology 2020Quote: ... Library preparation was carried out as described in the Illumina Nextera XT Sample Preparation Guide (Illumina, Inc., San Diego, CA, USA). 150 pg of input cDNA were tagmented (tagged and fragmented ...
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bioRxiv - Cell Biology 2021Quote: Sample libraries were prepared for Illumina sequencing by denaturing and diluting the libraries per manufacturer’s protocol (Illumina, San Diego, CA, USA). All samples were pooled into one sequencing pool ...
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bioRxiv - Genomics 2021Quote: ... Genome-wide SNP genotyping data were generated from the same samples using the “Global Screening Array” (GSA) with shared custom content (Illumina, Inc.) using procedures outlined in Hong et al ...
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bioRxiv - Genomics 2021Quote: ... and 750 ng per sample of bisulfite (BS)- or oxidative bisulfite (oxBS)-converted DNA was run on Infinium HumanMethylationEPIC (EPIC) BeadChips (Illumina Inc.) according to the manufacturer’s instructions ...
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bioRxiv - Genomics 2020Quote: ... Libraries were then barcoded and pooled into two lanes (eight samples in one and two in another) to generate 100bp paired-end reads on the HiSeq1500 sequencer (Illumina, Inc.).